BIOPSY SCISSORS
K-Number: K942030 · 1994-06-27
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Device Summary
Frequently Asked Questions
What is the BIOPSY SCISSORS?
BIOPSY SCISSORS is a medical device that received FDA 510(k) clearance on 1994-06-27. The listed applicant is Surgical Technologies, Inc.. The 510(k) number is K942030.
When did BIOPSY SCISSORS receive FDA 510(k) clearance?
BIOPSY SCISSORS received FDA 510(k) clearance on 1994-06-27, under 510(k) number K942030.
Who is the listed applicant for BIOPSY SCISSORS?
The FDA 510(k) record lists Surgical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIOPSY SCISSORS?
The FDA product code for BIOPSY SCISSORS is OCZ.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Surgical Technologies, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: OCZ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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